1152035-05-6

Basic information

• Product Name: 2-(3-Bromophenyl)-N-(tert-butyl)imidazo[1,2-a]pyridin-3-amine
• Synonyms: 2-(3-Bromophenyl)-N-(tert-butyl)imidazo[1,2-a]pyridin-3-amine
• CAS NO: 1152035-05-6
• Molecular Weight: 344.254
• Mol File: 1152035-05-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-(3-Bromophenyl)-N-(tert-butyl)imidazo[1,2-a]pyridin-3-amine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(3-Bromophenyl)-N-(tert-butyl)imidazo[1,2-a]pyridin-3-amine(1152035-05-6)
• EPA Substance Registry System: 2-(3-Bromophenyl)-N-(tert-butyl)imidazo[1,2-a]pyridin-3-amine(1152035-05-6)

Safety Data

• Hazardous Substances Data: 1152035-05-6(Hazardous Substances Data)

Upstream product

• 504-29-0 2-aminopyridine 
• 3132-99-8 m-bromobenzoic aldehyde 
• 119072-55-8 tert-butylisonitrile 

Downstream Products

• 504-29-0 2-aminopyridine 
• 1218939-10-6 2-(3-Bromophenyl)-N-(tert-butyl)-2-oxoacetamide 
• 5336-24-3 1,3-di-tert-butylurea 
• 75-64-9 tert-butylamine 

Relevant articles and documents

Diverse Oxidative C(sp2)-N Bond Cleavages of Aromatic Fused Imidazoles for Synthesis of α-Ketoamides and N-(pyridin-2-yl)arylamides

An efficient and chemoselective C(sp2)-N bond cleavage of aromatic imidazo[1,2-a]pyridine molecules is developed. A broad scope of amide compounds such as α-ketoamides and N-(pyridin-2-yl)arylamides are afforded as the final products in up to quantitative yields. Diverse C-N bond cleavages are controlled by the oxidative species used in this transformation, with various amide products afforded in a chemoselective fashion. A preliminary study indicated that some α-ketoamides exhibit anti-Tobacco Mosaic Virus activity for potential use in plant protection.